Case Report: Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: A novel mutation in a Turkish patient with glutaric aciduria type I

✍ Scribed by C. Mühlhausen; E. Christensen; M. Schwartz; N. Muschol; K. Ullrich; Z. Lukacs

• Book ID: 111574674
• Publisher: Springer
• Year: 2003
• Tongue: English
• Weight: 40 KB
• Volume: 26
• Category: Article
• ISSN: 0141-8955
• DOI: 10.1023/b:boli.0000005604.90621.e2